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Metachromatic leukodystrophyMucolipidosisSynucleinopathyI-cell diseaseMelas syndromeFamilial multiple lipomatosisGaucher's diseaseLysosomal storage diseaseFamilial amyloid polyneuropathyLipodystrophyDysplastic nevus syndromeCystinosisRefsum diseaseHurler syndromeTuberous sclerosisLipoprotein lipase deficiencyAa amyloidosisSanfilippo syndromeMucopolysaccharidosisKrabbe diseaseFamilial hypercholesterolemiaMotor neuron diseaseLysosomal acid lipase deficiencyLupus erythematosusSpinocerebellar ataxiaLeigh syndromeNeurosarcoidosisLewy bodyNeurodegenerative diseaseSclerodermaLeukoencephalopathyCancer syndromePhakomatosisSphingolipidosesMultiple endocrine neoplasiaMixed connective tissue diseaseAmyloidosisSystemic sclerodermaGlycogen storage diseaseNeurofibromatosis type iiTauopathyGlycogen storage disease type iiLupusLaminopathyMorquio syndromeSevere combined immunodeficiencyTyrosinemia type iGlycogen storage disease type iiiCorneal dystrophyAbetalipoproteinemiaCanavan diseasePycnodysostosisAutoimmune polyendocrine syndromeFerroptosisAutoimmune hepatitisAlexander diseaseHereditary elliptocytosisCirrhosisHyperimmunoglobulin e syndromeHistiocytosisNeuroacanthocytosisAmyloid plaquesPyruvate dehydrogenase deficiencyNecrobiosis lipoidicaNeurofibromatosis type iCentral nervous system diseaseParkinson-plus syndromeHunter syndromeMultiple system atrophyNeurodevelopmental disorderGranulomatosis with polyangiitisAlcoholic liver diseaseCohen syndromeGlycogen storage disease type vHippocampal sclerosisGlycogen storage disease type iMastocytosisSarcoidosisLymphoproliferative disordersMuscular dystrophyHereditary haemochromatosisNeurofibrillary tangleHereditary spherocytosisBinswanger's diseaseLipomatosisHartnup diseaseOpsoclonus myoclonus syndromeDiabetesMethylmalonic acidemiaPorphyriaCerebral amyloid angiopathyFamilial adenomatous polyposisCowden syndromeAstrogliosisFamilial dysbetalipoproteinemiaNon-alcoholic fatty liver diseaseOrganic acidemiaChronic granulomatous diseaseAlkaptonuriaDiffuse neonatal hemangiomatosis